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Adverse Events with a Frequency 5% Regardless of Causality by Body System Postmarketing Experience The following adverse reactions have been reported: Neurologic Reactions: Seizures have been reported to occur in patients, with or without pre-existing seizure activity, receiving either oral or intravenous levocarnitine

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Postnatal Strategy: A randomized controlled trial enrolled preterm infants (2836 weeks gestation) diagnosed with RDS within 6 h of birth
